Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/18—Manufacture of films or sheets
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/04—Oxygen-containing compounds
  • C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/16—Nitrogen-containing compounds
  • C08K5/20—Carboxylic acid amides
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
  • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
  • C08L23/04—Homopolymers or copolymers of ethene
  • C08L23/08—Copolymers of ethene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L91/00—Compositions of oils, fats or waxes; Compositions of derivatives thereof
  • C08L91/06—Waxes
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
  • C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
  • C08J2323/04—Homopolymers or copolymers of ethene
  • C08J2323/08—Copolymers of ethene
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
  • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
  • C08L23/04—Homopolymers or copolymers of ethene
  • C08L23/08—Copolymers of ethene
  • C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing other atoms than carbon or hydrogen atoms
  • C08L23/0853—Vinylacetate

Definitions

• This invention relates to an ethylene/vinyl acetate copolymer composition. More particularly, the invention relates to an ethylene/vinyl acetate copolymer synergistically compounded to provide anti-blocking characteristics.
• thermoplastic films such as ethylene/vinyl acetate copolymers tend to moisture fog as well as block.
• Both anti-blocking/anti-fogging properties of a film is necessary if it is used for packaging which contain water or moisture. particularly where such packages are subjected to temperature changes. Poor moisture antifog properties are especially undesirable, for example, in packaging of fresh meat products.
• Minimal haze, or maximum visible light transmission, is also a required property for many commercial applications in addition to antiblock and antifog properties.
• thermoplastic composition which comprises an ethylene/vinyl acetate copolymer admixture with a small amount of a mixture which comprises stearamide, behenamide, stearic acid and paraffin wax having a softening point of about 45C to about 55C according to ASTM E28-58T.
• thermoplastic film of ethylene/vinyl acetate copolymer composition which comprises 100 parts by weight of an ethylene/vinyl acetate copolymer characterized by having a melt index in the range of about [.2 to about 20 grams/ minutes according to ASTM No.
• thermoplastic composition contains about 0.15 to about 3 total parts by weight of about 0.02 to about 1 part by weight of individual modifiers selected Parts by weight per Modifier 100 parts copolymer Stearamide .02-l Behenamide .02l Stearic acid .02-l Paraffin Wax ,02-1
• thermoplastic composition of this invention is typically in the form of a film having a thickness of about 0.2 to about 10 mils and characterized by having an antiblock property according to antiblock test No. l, hereinafter described, of about 2 to about 30 grams, an antifog property of about 0 to about 0.5 minute at about 60C and a percent haze according to ASTM No. D 1003 of about 0 to about 10.
• ethylene/vinyl acetate copolymers can be prepared by polymerizing ethylene and vinyl acetate with various catalysts such as non-metallic catalysts, metal oxide catalysts and metal alkyl-reducible metal halide catalysts.
• catalysts include molecular oxygen, various peroxides, azo-bisisobutyronitrile, chromium oxide containing hexavalient chromium, alumina, thoria, zirconia, as well as the well-known organic metallic, particularly organoaluminum and organoaluminum halide Zeigler type catalysts.
• the ethylene and vinyl acetate monomers are polymerized at various temperatures in the range of about l00C to about 260C at pressures in the range of about 50 to about 50,000 pounds per square inch at residence times in the range of about 1 minute to about 4 hours, depending substantially upon the position of these reaction condition variables as well as the catalyst system. Further, depending on such variables, the polymerization reaction can be conducted in a solvent or in the absence of solvents and thus in the liquid or gaseous phase. By varying the catalyst system as well as the polymerization temperature time and pressure, the molecular weight, as evidenced by its melt index and density, of the thermoplastic copolymer can be controlled.
• the ethylene/vinyl acetate copolymer composition can be prepared by dissolving the required modifiers in an organic solvent at a temperature in the range of about 40C to about C followed by mixing therewith, the ethylene/vinyl acetate copolymer. The mixture is then dried by evaporating the organic solvent to yield the required composition. Typically, the mixture can be dried at a temperature of about 40C to about 150C depending primarily upon the organic solvent used. It should be readily understood that if the composition is to be dried as a film, substantially reduced temperatures and times can be used such as temperature in the range of about 70C to about C for a period of about 15 to about 60 minutes.
• EXAMPLE 1 A series of films was prepared by dispersing and dissolving an ethylene/vinyl acetate copolymer and modifying materials in benzene at about 50C to about 56C using a low-speed, laboratory air stirrer and then casting the solutions on glass plates. The cast polymer solution was partially dried on the plates in a plate oven at about 50C. The partially dried films were then completely dried in a dynamic air oven at 78C for about 40 minutes to provide a tough transparent film having a thickness of about 1 mil.
• the block test No. 2 is accomplished by first placing two film samples together so that a 5 inch X 5 inch 2-p1y specimen is obtained. This specimen is placed between two metal plates in a position and a 0.5 pounds per square inch pressure is exerted evenly over the entire plate. The assembly is placed in a dynamic hot air oven at 50C for 24 hours and then tested for block (sticking or adhesion) resistance.
• the antifog test is conducted by taut extension of the film over a beaker of hot water (60C), allowing about one inch of head space above the water. The time required for the moisture to be dispersed evenly over the film as a clear filament is recorded.
• Formulations l. 2. 3. and 4 are controls using individual modifying compounds Films of each of the Formulations l-9 were submitted to two antiblock tests and one moisture antifog test.
• the antiblock tests No. l and No. 2 are a measure of the force in gram required to separate films from another test film and the antifog test is expressed as the time requir'ed to disperse condensed water vapor on the film.
• Results of these antiblock and antifog tests of 40 tions of the modifying agents co-act to surprisingly provide a film having the required combination of antiblock and antifog properties as well as a clear film with little haze. Indeed, it was found that, for an optimum balance of properties, a combination of all four modifyfilms prepared according to Formulations l-9 are more ing agents is desirable.
• Table 2 further illustrates clearly shown in Table 2.
• the fatty acid amides are the stearamide which has the substantial following formula and the behenamide having the following substantial formula cant-c:
• thermoplastic composition which comprises lOO parts by weight of an ethylene/vinyl acetate copolymer, characterized by having a melt index in the range of about L2 to about 20 grams/ten minutes according to ASTM No. D 1238, resulting from the reaction of about 72 to about 80 parts by weight ethylene and, correspondingly, about 28 to about 20 parts by weight vinyl acetate wherein said thermoplastic composition contains about 0. 15 to about 3 total parts of a combination containing about 0.02 to about I part by weight of each individual modifier. said combination selected from l) stearamide and behenamide. (2) stearamide, behenamide and stearic acid.
• thermoplastic composition of claim 1 in the form of a film having a thickness of about 0.2 to about mils, an antiblock property according to antiblock test No. 1 of about 2 to about 30 grams, an antifog property of about 0 to about 0.5 minute at about C and a percent haze according to ASTM D 1003 of about 0 to about l0.
• thermoplastic composition of claim 2 in the form of said film where the modifier combination is stearamide, behenamide, stearic acid and paraffin wax.
• thermoplastic composition is dioxane and tetrahydrofuran. 4
• thermoplastic composition according to claim While certain representative embodiments and details have been shown for the purpose of illustrating the invention, it will be apparent to those skilled in this art that various changes and modifications may be made therein without departing from the spirit or scope of the invention.

Landscapes

• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Manufacturing & Machinery (AREA)
• Materials Engineering (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Manufacture Of Macromolecular Shaped Articles (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Wrappers (AREA)

Priority Applications (7)

Applications Claiming Priority (1)

Publications (1)

Family

ID=23847625

Family Applications (1)

Country Status (7)

Cited By (16)

Citations (3)

Family Cites Families (5)

• 1974
  • 1974-04-29 US US465391A patent/US3891587A/en not_active Expired - Lifetime
• 1975
  • 1975-04-01 CA CA223,536A patent/CA1038515A/en not_active Expired
  • 1975-04-07 GB GB1415775A patent/GB1467104A/en not_active Expired
  • 1975-04-07 DE DE2515059A patent/DE2515059C2/de not_active Expired
  • 1975-04-25 JP JP5061575A patent/JPS5615663B2/ja not_active Expired
  • 1975-04-28 FR FR7513257A patent/FR2309592A1/fr active Granted
  • 1975-04-28 IT IT22778/75A patent/IT1037665B/it active

Patent Citations (3)

Also Published As

Similar Documents

Legal Events